Aquaporin-4-dependent glymphatic solute transport in the rodent brain

Humberto Mestre(University of Rochester Medical Center), Lauren M. Hablitz(University of Rochester Medical Center), Anna LR Xavier(University of Copenhagen), Weixi Feng(Nanjing Medical University), Wenyan Zou(Nanjing Medical University), Tinglin Pu(Nanjing Medical University), Hiromu Monai(Ochanomizu University), Giridhar Murlidharan(University of North Carolina at Chapel Hill), Ruth M. Castellanos Rivera(University of North Carolina at Chapel Hill), Matthew Simon(Oregon Health & Science University), Martin M. Pike(Oregon Health & Science University), Virginia Plá(University of Rochester Medical Center), Ting Du(University of Rochester Medical Center), Benjamin T. Kress(University of Rochester Medical Center), Xiaowen Wang(RIKEN Center for Brain Science), Benjamin A. Plog(University of Rochester Medical Center), Alexander S. Thrane(University of Copenhagen), Iben Lundgaard(Lund University), Yoichiro Abe(Keio University), Masato Yasui(Keio University), John H. Thomas(University of Rochester), Ming Xiao(Nanjing Medical University), Hajime Hirase(RIKEN Center for Brain Science), Aravind Asokan(University of North Carolina at Chapel Hill), Jeffrey J. Iliff(Oregon Health & Science University), Maiken Nedergaard(University of Copenhagen)
eLife
December 18, 2018
Cited by 721Open Access
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Abstract

The glymphatic system is a brain-wide clearance pathway; its impairment contributes to the accumulation of amyloid-β. Influx of cerebrospinal fluid (CSF) depends upon the expression and perivascular localization of the astroglial water channel aquaporin-4 (AQP4). Prompted by a recent failure to find an effect of Aqp4 knock-out (KO) on CSF and interstitial fluid (ISF) tracer transport, five groups re-examined the importance of AQP4 in glymphatic transport. We concur that CSF influx is higher in wild-type mice than in four different Aqp4 KO lines and in one line that lacks perivascular AQP4 (Snta1 KO). Meta-analysis of all studies demonstrated a significant decrease in tracer transport in KO mice and rats compared to controls. Meta-regression indicated that anesthesia, age, and tracer delivery explain the opposing results. We also report that intrastriatal injections suppress glymphatic function. This validates the role of AQP4 and shows that glymphatic studies must avoid the use of invasive procedures.


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